Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Luca Pasquinelli"'
Autor:
Elisabetta Rosadoni, Federico Banchini, Sara Bellini, Marco Lessi, Luca Pasquinelli, Fabio Bellina
Publikováno v:
Molecules, Vol 27, Iss 23, p 8454 (2022)
The palladium-catalyzed direct arylation of azoles with (hetero)aryl halides is nowadays one of the most versatile and efficient procedures for the selective synthesis of heterobiaryls. Although this procedure is, due to its characteristics, also of
Externí odkaz:
https://doaj.org/article/bf176997c3924bd28309e5cd8d308e0c
Autor:
Matteo Pollastrini, Luca Pasquinelli, Marcin Górecki, Federica Balzano, Lorenzo Cupellini, Filippo Lipparini, Gloria Uccello Barretta, Fabio Marchetti, Gennaro Pescitelli, Gaetano Angelici
Publikováno v:
The Journal of Organic Chemistry. 87:13715-13725
Polyproline I helical structures are often considered as the hidden face of their most famous geminal sibling, Polyproline II, as PPI is generally spotted only within a conformational equilibrium. We designed and synthesized a stable Polyproline I st
Autor:
Matteo, Pollastrini, Filippo, Lipparini, Luca, Pasquinelli, Federica, Balzano, Gloria Uccello, Barretta, Gennaro, Pescitelli, Gaetano, Angelici
Publikováno v:
The Journal of Organic Chemistry
A thorough experimental and computational study on the conformational properties of (S)-indoline-2-carboxylic acid derivatives has been conducted. Methyl (S)-1-acetylindoline-2-carboxylate, both a mimetic of proline and phenylalanine, shows a remarka
Autor:
Gennaro Pescitelli, Gloria Uccello Barretta, Matteo Pollastrini, Gaetano Angelici, Filippo Lipparini, Luca Pasquinelli, Federica Balzano
A thorough experimental and computational study on the conformational properties of (S)-indoline-2-carboxylic acid derivatives has been conducted. Methyl (S)-1-acetylindoline-2-carboxylate, both a mimetic of proline and phenylalanine, shows a remarka
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d12ffd3280a018eee494e5f862493884
http://hdl.handle.net/11568/1102718
http://hdl.handle.net/11568/1102718